Hao Kai, Zhu Xueliang, Yan Xiumin
State Key Laboratory of Cell Biology, Shanghai Institute of Biochemistry and Cell Biology, Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences, 320 Yueyang Road, Shanghai 200031, China.
University of Chinese Academy of Sciences, Beijing 100049, China.
Bio Protoc. 2022 Jul 20;12(14). doi: 10.21769/BioProtoc.4467.
Cilia and flagella are microtubule-based hair-like organelles protruding from the surface of most eukaryotic cells, and play essential roles in cell locomotion, left-right asymmetry, embryo development, and tissue homeostasis. With isolated cilia and flagella, great progress has been made in understanding the composition, structure, and function of cilia. However, the current cilia/flagella isolation methods are deficient in the integrity or productivity of purified cilia when applied to mammalian motile cilia. Here, we describe a new protocol that isolates cilia shafts from mouse ependymal cells, by horizontal shear force and mild detergent. This method enables the production of virtually integral cilia with high yields and less cell body contamination. It is suitable for immunostaining, puromycin labeling assay, and proximity ligation assay of mammalian motile cilia. Graphical abstract.
纤毛和鞭毛是基于微管的毛发状细胞器,从大多数真核细胞表面突出,在细胞运动、左右不对称、胚胎发育和组织稳态中发挥重要作用。借助分离出的纤毛和鞭毛,在了解纤毛的组成、结构和功能方面取得了巨大进展。然而,当前的纤毛/鞭毛分离方法在应用于哺乳动物运动性纤毛时,纯化纤毛的完整性或产量存在不足。在此,我们描述了一种新方法,通过水平剪切力和温和去污剂从小鼠室管膜细胞中分离纤毛轴。该方法能够以高产率生产几乎完整的纤毛,且细胞体污染较少。它适用于哺乳动物运动性纤毛的免疫染色、嘌呤霉素标记测定和邻近连接测定。图形摘要。